Vulcanization retarders

ABSTRACT

N,N&#39;&#39;-thio-bis-carbamic acid amides, their preparation by reacing at least 2 mols of a carboxylic acid amide with 1 mol of sulphur dichloride in the presence of an acid binding agent and their utility as rubber vulcanization retarders.

United States Patent Schubart et a1. [4 June 20, 1972 [54] VULCANIZATION RETARDERS [58] Field of Search ..260/780, 79.5 B, 545, 239 B, [72] Inventors: Rudiger Schubart; Ernst Roos, both of 260/294'7 326's 782 Cologne: Manfred Abele, Porz, all of Ger- [56] References cued many [73] Assignee: Farbeniabrlken Bayer Aktlengesellschaft, UNITED STATES PATENTS Level'kusen, Germany 3,546,185 12/1970 Coran ..260/79.5 B

[22] Flled: 1970 Primary Evaminer--James A. Seidleck [21] Appl. No.: 90,859 Assistant Examiner-C. A. Henderson, .Ir.

Attorney-Connolly and Hut:

[301 Foreign Application Priority Data 57] ABSTRACT Dec. 13, 1969 Germany ..P 19 62 604.1 N,NI thio bis carbamic acid amides their preparation by reacing at least 2 mols of a carboxylic acid amide with 1 mol of [52] U.S.Cl. ..260/79.5 B, 260/239 B, 260/294.7, sulphur dichloride in the presence f an i i i agent 260/326.8 260/545 R, 260/780, 260/782, 2265477 84; and their utility as rubber vulcanization retarders [51 Int. Cl ..C08f 27/06, C080 1 H60, C08c 1 1/54 4 Claims, No Drawings VULCANIZATION RETARDERS The present invention relates to the use of N,N'-thio-biscarboxylic acid amides as vulcanization retarders in the production and processing of mixtures based on natural or synthetic rubber. The invention also relates to new N,N'-thiobis-carboxylic acid amides and their preparation.

In the production and processing of rubber mixtures which contain vulcanizing agents, e.g. sulphur and accelerators, a certain amount of premature vulcanization, known as scorching, may occur before the proper vulcanization (see Bayer-Mitteilungen fur die Gummie-lndustrie, No. 42 of 1.5.1968, pages 3 7, in particular page 3, left-hand column). This scorching may occur, for example, in the mixer or during any of the subsequent processes such as extruding or calendermg.

' It is known that the risk of scorching can be reduced by the addition of a N-nitrosoamine, especially N-nitroso-diphenylamine, to the rubber mixture (see Technical Information R 22 Rubber Chemicals" of Imperial Chemical Industries, Manchester, England, paper 1 ll, in particular page 1; Rubber Chemistry and Technology, Vol. 30 (1957), pages 1,291 1,346, in particular page l302, lines 3 and 4; Rubber Journal, March 1967, page 1 l, right-hand column, paragraph 2, in particular line 18 of the right-hand column).

In certain circumstances, however, the use of these retarders leads to the formation of .porous vulcanizates due to the nitroso group being split off (see Technical Information R 22 Rubber Chemicals of Imperial Chemical Industries, Manchester, England, pages 1 ii, in particular page 2, second paragraph). Furthermore, these compounds not only influence the scorching but also have a marked effect on the entire vulcanization process, i.e. the vulcanization time is increased (see Bayer Mitteilungen fur die Gummi-lndustrie, No. 42 of 1.5.1968, pages 3 7, in particular page 3, right-hand column, lines 39 45, and page 3, right-hand column, last paragraph, in particular lines 47, 48, 55 and 56).

Furthermore, a rather large dose of an N-nitrosoamine is required for achieving a given retarding effect.

It has now been found that N,N'-thio-bis-carboxylic acid amides of the general formula:

in which R and R, independently of each other represent hydrogen or an alkyl radical, a cycloalkyl radical, an aryl radical optionally substituted by one or more alkyl groups, or an aralkyl radical, and together may form a carbocyclic ring having up to l2 carbon atoms, are suitable for use as vulcanization retarders in the known methods of producing and processing mixtures which contain natural or synthetic rubber.

The N,N-thio-bis-carboxylic acid amides surprisingly show a substantially more powerful effect as vulcanization retarders than the N-nitrosoamines known in the art. Moreover, they do not give rise to porous vulcanizates and, when used in suitable quantities, they have less influence on the time required for complete vulcanization than have N-nitrosoamines.

The following are examples of radicals R and R in the formula (I): unbranched or branched alkyl groups having from one to six carbon atoms, such as methyl, ethyl, n-propyl, isopropyl, n-butyl, secondary butyl, isobutyl, tertiary butyl, npentyl, isoamyl, n-hexyl; the cyclohexylmethyl radical; cycloalkyl groups such as cyclopentyl, cyclohexyl or methylcyclohexyl; aralkyl groups such as benzyl, phenylethyl, phenylpropyl or phenylisopropyl. The following are mentioned as examples of aryl radicals R and R which may be substituted by alkyl groups: phenyl, a-naphthyl, methylphenyl, ethylphenyl, n-propylphenyl, isopropylphenyl, n-butylphenyl or tertiary butylphenyl, any of the previously mentioned alkyl groups being either in the orthometaor para-position of the phenyl radical; also, 2,3-dimethylphenyl, 2,4-dimethylphenyl, 2,5- dimethylphenyl, 2,6-dimethylphenyl, 3,5-dimethylphenyl, 3,4-

dimethylphenyl, 2,3-diethylphenyl, 2,4-diethylphenyl, 2,5- diethylphenyl, 2,6-diethylphenyl, 3,4-diethylphenyl, 3,5- diethylphenyl, 2-methyl-3-ethylphenyl, 2-methyl-4-ethylphenyl, 2-methyl-5-ethylphenyl, 2-methyl-6-ethylphenyl, 3-methyl- 2-ethylphenyl, 3-methyl-4-ethylphenyl, 3-methyl-5-ethylphenyl, 4-methyl-2-ethylphenyl, 4-methyl-3-ethylphenyl, S-methyl- 2-ethylphenyl, 2,3,4-trimethylphenyl, 3,4,6-trimethylphenyl,

triethylphenyl, 2,3,6-triethylphenyl, 2,4,5-triethylphenyl, 2,4,6-triethylphenyl and 3,4,5-triethylphenyl.

The following are mentioned as specific examples of compounds which may be used for the invention: N,N'-thio-bisformamide, N,N'-thio-bis-acetamide, N,N-thio-bis-propionamide, N,N'-thio bis-(N-methylformamide), N,N'-thio-bis-(N- methyl acetamide), N,N-thio-bis-(n-ethyl acetamide), N,N'- thio-bis-(N-propyl acetamide), N,N-thio-bis-(N-methyl propionamide), N,N-thiobis-(N-ethyl propionamide), N,N'- thio-bis-(N-methyl butyric acid amide), N,N-thio-bis-(N- ethyl butyric acid amide), N,N'-thio-bis-(N-methyl isobutyric acid amide), N,N'-thio-bis-(N-ethyl isobutyric acid amide), N,N'-thio-bis-(N-methyl pentane carboxylic acid amide), N,N'-thio-bis-(N-cyclohexyl methyl acetamide), N,N'-thiobis-(N-cyclopentyl acetamide), N,N'-thio-bis-(N-cyclohexyl acetamide), N,N'-thio-bis-( N-methyl cyclohexyl acetamide),

N,N'-thio-bis-(benzyl acetamide), N,N'-thio-bis-(N-benzyl formamide), N,N'-thio-bis-(N-phenylethyl acetamide), N,N'- thio-bis-(N-phenyl formamide), N,N'-thio-bis-(N-phenyl acetamide), N,N-thio-bis-(N-a-naphthyl acetamide), N,N'- thio-bis-(N-4-methylphenyl acetamide), N,N-thio-bis-(N-4- ethylphenyl acetamide), N,N'-thio-bis-(N-Z-methylphenyl acetamide), N,N-thio-bis-(N-2-ethylpehnyl acetamide), N,N-thio-bis-(N-2,3-dimethylphenyl acetamide), N,N'-thiobis-( N-2,4-dimethyl-phenyl acetamide), N,N'-thio-bis-( N-2,6- dimethylphenyl acetamide), N,N-thio-bis-(N-2,5- diethylphenyl acetamide), N,N'-thio-bis-(N-3,4-diethylphenyl acetamide), N,N'-thio-bis-(N-2-methyl-4-ethylphenyl acetamide), N,N-thio-bis-(N-4-methyl-3-ethylphenyl acetamide), N,N-thio-bis-(N-2,3,4trimethylphenyl acetamide), N,N'- thio-bis-(N-2,4,6-trimethylphenyl acetamide), N,N'-thio-bis- (N-phenylpropionamide N,N'-thio-bis-( N-2-methylphenyl propionamide), N,N-thio-bis-(N-benzyl propionamide), N,N'-thio-bis-(N-phenyl butyric acid amide), N,N-thio-bisbenzamide, N,N-thio-bis-(N-methyl benzamide), N,N'-thiobis-(N-ethyl benzamide), N,N'-thio-bis-(N-propyl benzamide), N,N'-thio-(N-cyclohexyl benzamide), N,N-thio-bis- (N-cyclopentyl bemzamide N,N-thio-bis-( N-methylcyclohexyl benzamide), N,N-thio-bis-(N-phenylcyclohexane carboxylic acid amide), N,N'-thio-bis-(N-4-methylphenylcyclohexane carboxylic acid amide), N,N-thio-bis-(N-phenyl benzamide), N,N-thio-bis(N-4-methylphenyl benzamide), N,N-thio-bis-(N-Z-methylphenyl benzamide), N,N'-thio-bis- (N-3-methylphenyl benzamide), N,N'-thio-bis-(N-phenyl-4- methyl benzamide), N,N-thio-bis-(N-Z-rnethylphenylmethyl benzamide), N,N'-thio-bis-(N-phenyl-2,4,6-trimethyl benzamide), N,N'-thio-bis-(N-methyl-2,4,6-trimethyl benzamide), N,N'-thio-bis-(N-2-methylphenyl-2,4,-trimethyl benzamide), N,N'-thio-bis-(N-2,6-dimethylphenyl benzamide), N,N-thio-bis-(N-2,4,6-trimethylphenyl benzamide), N,N'-

thio-bis-(N-a-naphthyl benzamide), N,N-thio-bis-(N-B- naphthyl benzamide N ,N -thio-bis-( N-phenyl-a-naphthalene carboxylic acid amide), N,N-thio-bis-(N-a-naphthyl-anaphthalene carboxylic acid amide), N,N-thio-bis-(N-phenyla-naphthalene carboxylic acid amide) and N,N-thio-bis-(N- phenyl-a-naphthalene carboxylic acid amide). The following are examples of compounds of formula (I) where R and R form a carbocyclic ring: N,N'-thio-bis-pyrrolidine-2; N,N- thio-bis-caprolactam; N,N-thio-bis-piperidone-2 and N,N- thio-bis-dodecanelactam.

Suitable rubbers for the production and processing of mixtures based on natural or synthetic rubbers are, for example, natural rubber or synthetic rubber-like polymers which are obtained e.g. from conjugated diolefines such as butadiene, dimethylbutadiene, isoprene and its homologues, or copolymers of such conjugated diolefines with polymerizable vinyl compounds such as styrene, a-methyl styrene, acrylonitrile, methacrylonitrile, acrylates or methacrylates.

The retarders used according to the invention may be mixed with the rubber in the conventional manner, for example using mixing rollers or an internal mixer. They are preferably added before or together with the other constituents but they may also be added last. The amount of retarder according to the invention should preferably be from 0.05 to 5.0 percent by weight, and preferably from 0.1 to 1.5 percent by weight, based on the rubber.

The rubber mixtures to be treated contain, of course, the conventional additives required for vulcanization, such as vulcanizing agents and accelerators. The vulcanizing agent, e.g. sulphur, may be used in the conventional quantity for vulcanization, generally 0.2 to 5 .0 percent by weight of the rubber. Examples of suitable accelerators are thiazoles such as Z-mercaptabenzothiazole or benzothiazyl sulphenomorpholide, guanidines such as diphenyl guanidine or di-o-tolylguanidine, dithiocarbamates such as diethyldithiocarbamic acid zinc, and thiurams such as tetramethyl thiuramic disulphide or tetramethyl thiuramic monosulphide. Mixtures of accelerators may also be used. The accelerator is generally used in a quantity of from 0.05 to 5 percent by weight, preferably 0.05 to 2.5 percent by weight, and in particular 0.] to 1.5 percent by weight, based on the rubber.

The rubber mixture may also contain other known auxiliary substances, e.g. active or inactive fillers such as chalk or carbon black, antioxidants, antiozonants, waxes, pigments, zinc oxides, fatty acids such as stearic acid or processing oils.

'Vulcanization of the rubber may be carried out by heating the rubber to the usual temperatures, preferably to a temperature of from C. to 170 C., although higher or lower temperatures may also be employed.

The invention also relates to new N,N"thio-bis-carboxylic acid amides of the formula:

in which R and R, represent, independently of each other,

hydrogen or an alkyl radical, a cycloalkyl radical, an aryl radical which may be substituted by one or more alkyl groups, or an aralkyl radical.

The following are examples of the radicals R and R straight chained or branched alkyl groups having one to six carbon atoms, such as methyl, ethyl, npropyl, isopropyl, n-butyl, secondary butyl, isobutyl, tertiary butyl, n-pentyl, isoamyl, n-hexyl; the cyclohexylmethyl radical; cycloalkyl groups such as the cyclopentyl, cyclohexyl or methylcyclohexyl groups; aralkyl groups such as benzyl, phenylethyl, phenylpropyl or phenylisopropyl. The following are examples of suitable aryl radicals R and R optionally substituted by one or more alkyl groups: phenyl, a-naphthyl, methylphenyl, ethylphenyl, n-propylphenyl, isopropylphenyl, n-butylphenyl and tertiary butylphenyl, all these alkyl groups being either in the ortho-, metaor para-position of the phenyl radical; furthermore, 2,3- dimethylphenyl, 2,4-dimethylphenyl, 2,5-dimethylphenyl, 2,6-

dimethylphenyl, 3,5-dimethylphenyl, 3,4-dimethylphenyl, 2,3- diethylphenyl, 2,4 diethylphenyl, 2,5-diethylphenyl, 2,6- diethylphenyl, 3,4-diethylphenyl, 3,5-diethylphenyl, 2-methyl- 3-ethylphenyl, 2-methyl-4-ethylphenyl, 2-methyl-5-ethylphenyl, 2-methyl-6-ethylphenyl, 3-methyl-2-ethylphenyl, 3-methyl- 4-ethylphenyl, 3-methyl-5-ethylphenyl, 4-methyl-2-ethylphenyl, 4-rnethyl- 3-ethylphenyl, 5-methyl-2-ethylphenyl, 2,3,4- trimethylphenyl, 3,4,6-trimethylphenyl, 3,4,5-trimethylphenyl, 2,3-dimethyl-4-ethylphenyl, 2,3-dimethyl-5-ethylphenyl, 2,3-dimethyl-6-ethylphenyl, 2,4-dimethyl-3-ethylphenyl, 2,4- dimethyl-S-ethylphenyl, 2,4-dimethyl-6-ethylphenyl, 2,5-

dimethyl-S-ethylphenyl, 2,5-dimethyl-4-ethylphenyl, 2 ,5- dimethyl--ethylphenyl, 2,o-dimethyl-3-ethylphenyl, 2,6- dimethyl-4-ethylphenyl, 3 ,4-dimethyl-2-ethylphenyl, 3 ,4- dimethyl-S-ethylphenyl, 3 ,4-dimethyl-6-ethylphenyl, 3 ,5- dimethyl-4-ethylphenyl, 3 ,5-dimethyl-6-ethylphenyl, 4- methyl-2,3-diethylphenyl, 5-methyl-2,3-diethylphenyl, 6- methyLZJ-diethylphenyl, 3-methyl-2,4-diethylphenyl, 5 methyl-2,4-diethylphenyl, 6-methyl-2,4-diethylphenyl, 3' methyl-2,5-diethylphenyl, 4-methyl-2,5-diethylphenyl, 6- methyl-2,5-diethylphenyl, 3-methyl-2,6-diethylphenyl, 4- methyl-2 ,o-diethylphenyl, 2-methyl-3,4-diethylphenyl, 5 methyl-3 ,4-diethylphenyl, 6-methyl-3,4-diethylphenyl, 4-

methyl-3,5-diethylphenyl, 6-methyl-3,S-diethylphenyl, 2,3,4-

triethylphenyl, 2,3,5-triethylphenyl, 2,3,6-triethylphenyl, 2,4,5-triethylphenyl, 2,4,6-triethylphenyl and 3,4,5- triethylphenyl.

The following are specific examples of new compounds of the formula (II): N,N'-thio-bis-formamide, N,N'-thio-bisacetamide, N,N'-thio-bis-propionamide, N,N-thio-bis-(N- methyl formamide), N,N'-thio-bis-(N-methyl acetamide), N,N'-thio-bis-(N-ethyl acetamide), N,N'-thio-bis-(N-propyl acetamide), N,N-thio-bis-(N-methyl propionamide), N,N- thio'bis-(N-ethyl propionamide), N,N-thio-bis-(N-methyl butyric acid amide), N,N-thio-bis-(N-ethyl butyric acid amide), N,N-thiobis-(N-methyl isobutyric acid amide), N,N'-thiobis-(N-ethyl isobutyric acid amide), N,N-thio-bis-(N-methyl pentane carboxylic acid amide), N,N'-t.hio-bis-(N-cyclohexylmethyl acetamide), N,N-thio-bis-(N-cyclopentyl acetamide), N,N-thio-bis-(N-cyclohexyl acetamide), N,N-thio-bis-(N- methylcyclohexyl acetamide), N,N'thio-bis-( benzyl acetamide), N,N'-thio-bis-(N-benzyl formamide), N,N'-thio-bis- (N-phenylethylacetamide), N,N-thio-bis(N-phenyl formamide), N,N'-thio-bis-(N-phenyl acetamide), N,N'-thio-bis- (N-a-naphthyl acetamide), N,N' thio-bis-(N-4-methylphenyl acetamide), N,N-thio-bis-(N-4-ethylphenyl acetamide), N,N'-thio-bis-( N-2-ethylphenyl acetamide N,N '-thio-bis-( N- 2,3-dimethylphenyl acetamide N,N'-thio-bis-( N-2 ,4- dimethylphenyl acetamide N,N'-thio-bis-( N-2 ,6- dimethylphenyl acetamide N,N-thio-bis-( N-2,5

thio-bis-(N-a-naphthyl benzamide), N, N'-thio-bis-(N-B- naphthyl benzamide), N,N'-thio-bis-(N-phenyl-a-naphthalene carboxylic acid amide), N,N'thio-bis-(N-phenyl-B- naphthalene carboxylic acid amide), and N,N-thio-bis-(N-anaphthyLa-naphthalene carboxylic acid amide).

The new compounds of the formula (II) are prepared by reacting at least 2 mols of a carboxylic acid amide of the formula:

R1 2R'CO-I IH (III) wherein R and R, represent, independently of each other,

hydrogen or an alkyl radical, a cycloalkyl radical, an aryl radical, optionally substituted by one or more alkyl groups, or an aralkyl radical, with at least one mol of sulphur dichloride in the presence of an acid binding agent.

The reaction of a compound of the formula (III) with sulphur dichloride may be represented by the following reaction scheme:

The reaction is carried out at a temperature of from 50 C. to +50 C, preferably at l C, to lO C.

The quantities of the reactants used may vary within wide limits. If a liquid carboxylic acid amide of the formula (III) enters into the reaction, it may be advisable to use this component in excess, the carboxylic acid amide used then serving also as solvent. In general, however, the reactants are used in equimolecular quantities. If desired, an inert organic solvent or diluent may, of course, be used as the reaction medium. The following are examples of suitable solvents or diluents: hydrocarbons such as light fraction petroleum hydrocarbons, cleaning petrol, hexane, cyclohexane, benzene, toluene and xylene; chlorinated hydrocarbons such as methylene chloride, ethylene chloride, chloroform, carbon tetrachloride and chlorobenzene; ethers such as diethyl ether, diisopropyl ether, dioxane and tetrahydrofuran; ketones such as acetone, methyl ethyl ketone, diethyl ketone, methyl propyl ketone, methyl butyl ketone, di-n-propyl ketone, methylisopropyl ketone and cyclohexanol.

Both inorganic and organic bases are suitable for use as the acid binding agent. As a rule, the acid binding agent used is a tertiary amine such as triethylamine, N,N-dimethyl aniline and especially a pyridine base such as pyridine, an alkyl pyridine or quinoline, but an inorganic base such as magnesium oxide, sodium carbonate, potassium carbonate or calcium carbonate may also be used as the acid binding agent, in which case, it may be advantageous to add these compounds in a finely divided form. If the acid binding agent is a liquid compound, e.g. pyridine, it may, of course, also serve as a solvent or diluent.

The reactants may be added in any sequence. As a rule, carboxylic acid amide and the acid binding agent are introduced into the reaction vessel and sulphur dichloride, optionally dissolved in a solvent, is added thereto. The products are worked up in the usual manner, e.g. by removal of the resulting aminohydrochloride or inorganic chloride (if an inorganic base was used as the acid binding agent) by filtration or washing with water, followed by isolation of the N,N'-thio-bis-carboxylic acid amide. The new compounds are generally colorless, crystalline substances.

The following are examples of acid amides (III) which may be used for the reaction: fonnamide, acetamide, propiona mide, N-methyl formamide, Nmethyl acetamide, N-ethyl acetamide, N-propyl acetamide, N-methyl propionamide, N- ethyl propionamide, N-methyl butyric acid amide, N-ethyl butyric acid amide, N-methyl isobutyric acid amide, N-ethyl isobutyric acid amide, N-methyl pentane carboxylic acid amide, N-cyclohexylmethyl acetamide, N-cyclopentyl acetamide, N-cyclohexyl acetamide, N-methylcyclohexyl acetamide, N-benzyl acetamide, N-benzyl formamide, N-phenylethyl acetamide, N-phenyl formamide, N-phenyl acetamide, N-a-naphthyl acetamide, N-4-methylphenyl acetamide, N-4- ethylphenyl acetamide, N-2-methylphenyl acetamide, N-2- ethylphenyl acetamide, N-2,3-dimethylphenyl acetamide, N- 2,4-dimethyl phenyl acetamide, N-2,6-dimethylphenyl acetamide, N-2,5-diethylphenyl acetamide, N-3,4-diethylphenyl acetamide, N-2-methyl-4-ethylphenyl acetamide, N-4-methyl- 3-ethylphenyl acetamide, N2,3,4-trimethylphenyl acetamide, N-2,4,6-trimethylphenyl acetamide, N-phenyl propionamide, N-Z-methylphenyl propionamide, N-benzyl propionamide, N- phenyl butyric acid amide, benzamide, N-methyl benzamide, N-ethyl benzamide, N-propyl benzamide, N-cyclohexyl benzamide, N-cyclopentyl benzamide, N-methylcyclohexyl benzamide, N-phenyl cyclohexane carboxylic acid amide, N-4- methylphenyl-cyclohexane carboxylic acid amide, N-phenyl benzamide, N-4-methylphenyl benzamide, N2-methylphenyl benzamide, N-3-methylphenyl benzamide, N-phenyl-4-methyl benzamide, N-2-methylphenylmethyl benzamide, N-phenyl- 2,4,6-trimethylbenzamide, N-methyl-2,4,6-trimethyl benzamide, N-2-methylphenyl-2,4,6-trimethyl benzamide, N-2,6- dimethylphenyl benzamide, N-2,4,6-trimethylphenyl benzamide, N-a-naphthyl benzamide, N-B-naphthyl benzamide, N- phenyl-a-naphthalene carboxylic acid amide, N-a-naphthyl-anaphthalene carboxylic acid amide and N-phenyl-anaphthalene carboxylic acid amide.

The following Examples illustrate the invention. The values shown in the tables are parts by weight, based on 100.0 parts by weight of the rubber.

The test methods are defined as follows (see also Kautschuk und Gummi; Kunststoife 20, No. 3/1967, pages 126 134, in particular pages 127 and 133):

Scorch time: In analogy with the Mooney Scorch time (see DIN 53 524), time determined from the tension/heating time curve until the tension rises by 20 points above the minimum at 300 percent elongation (stepwise vulcanization at C).

M 300: Tension (kg wt/cm) at 300 percent elongation according to DIN 53 504, sheet 2.

F: Tensile strength (kg wtlcm according to DIN 53 504.

sheet 1, Standard ring R l.

D: Elongation at break according to DIN 53 504 sheet 1 Standard ring R I.

H: Hardness (Shore A), DIN 53 505, range A, 4 mm flaps.

Complete vulcanization time: Time taken to reach 90 percent of the maximum tension (at 300 percent elongation at C.

EXAMPLE 1 The following mixtures were prepared on mixing rollers: v

Mixture No 1 2 3 4 5 Natural rubber, smoked shunts 100.0 100. (1 100. 0 100.0 100.0 Zinc oxide 5. 0 5. 0 5. 0 5. 0 5. 0 Stearic acid 3. 0 3.0 3.0 3.0 3.0 Aromatic mineral oil plasticiser 2. 5 2. 5 2.5 2. 5 2.5 High abrasion furnace black 45. l) 45. 0 45. 0 45. 0 45. 0 Naplithenie mineral oil plasticisen 2. 5 2. 5 2. 5 2. 5 2. 5 Sulphur 2. 3 2. 3 2. 3 2. 3 2. 3 N-c vvloliexy i-2-benzothiazyl sulphenain de 0.5 0.5 0.5 0.5 0.5 N-mtrosodi ienylaniine (for compari- SO 0. 6 N, N"tl1io-l)is-(N-pliunyl aoctnmido) 0. 2 N. N-hispyrrol i(l0n-('.2)-sulpl1id0 0. 3

The mixtures obtained were vulcanised under pressure to produce test samples 4 mm. in thickness, heating being carried out stepwise at 110 C. and 140 C. The results shown in Table I were obtained.

TAB LE I Mechanleal values corresponding to the Complete complete vulcanisatlon time Scorch vulcanisatime at tion time F M 300 lvlrxture 110 C. at 140 0. (kg. wt./ D (kg. wt./ II No. Scorch retarder (min.) (min em?) (percent) em!) (Shore A) None 63. 22. 240 550 105 61 N-nrtroso-drphenylamlne (for comparison 84. 5 28. 3 220 560 17 N ,N-thlo-bls-(N -pher1yl acetamide) 83. 5 24. 4 210 500 108 2 N,N-th1o-bis-(pyrr0l1done-2) s5. 0 24. 9 230 510 112 62 N,N-th1o-b1s-(caprolactam) 83.0 24. 2 236 530 110 63 EXAMPLE 2 CH3(|3N- SI I-fiCHa When the amides listed under A in the following Table 11 are used instead of N-phenyl acetamide, the compounds shown under B are obtained.

vantageous influence of the compounds used according to the invention on the vulcanization characteristic.

What is claimed is:

1. A process for vulcanizing natural rubber or a synthetic rubber based on a conjugated diolefin which comprises incorporating in said rubber, as vulcanizing agent, sulphur and, as a vulcanization retarder, 0.05 to 5.0 percent by weight, based on the weight of the rubber, of a compound of the formula wherein R and R, are, independently of each other, hydrogen, alkyl having from one to six carbon atoms, cyclohexylmethyl. cycloalkyl having from five to seven carbon atoms, phenylalkyl having from one to three carbon atoms in the alkyl moiety, phenyl, a-naphthyl, monoalkylphenyl having from one to four carbon atoms in the alkyl moiety, dialkylphenyl having from 1 to 2 carbon atoms in each alkyl moiety and trialkylphenyl having from one to two carbon atoms in each alkyl moiety or R and R together form an alkylene bridge containing 3 or 5 carbon atoms and heating resulting mixture to a temperature of TABLE II Melting A B CH1 132-131 (i=0 0 CH3 -66 curb- 1bit us I 0 on; 'i ll lli (H) 134436 /\N1I It will be seen added a dose and 0.3 percent by weight, respectively, based on 100.0 parts by weight of rubber, have the same retarding effect as N- nitrosodiphenylamine added in an amount of 0.6 percent by weight. It follows, therefore, that the new retarclers are at least twice as effective and in some cases even more so (see Table 11).

ewe-un said vulcanization re- 

2. The process of claim 1 wherein said vulcanization retarder is N,N''-thio-bis-(N-phenyl acetamide).
 3. The process of claim 1 wherein said vulcanization retarder is N,N''-thio-bis-(pyrrolidone-2).
 4. The process of claim 1 wherein said vulcanization retarder is N,N''-thio-bis-(caprolactam). 